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Transformer-based de novo peptide sequencing for data-independent acquisition mass spectrometry.
Ebrahimi, Shiva; Guo, Xuan.
Afiliação
  • Ebrahimi S; Computer Science & Engineering, University of North Texas, Denton, USA.
  • Guo X; Computer Science & Engineering, University of North Texas, Denton, USA.
ArXiv ; 2024 Jun 26.
Article em En | MEDLINE | ID: mdl-38659639
ABSTRACT
Tandem mass spectrometry (MS/MS) stands as the predominant high-throughput technique for comprehensively analyzing protein content within biological samples. This methodology is a cornerstone driving the advancement of proteomics. In recent years, substantial strides have been made in Data-Independent Acquisition (DIA) strategies, facilitating impartial and non-targeted fragmentation of precursor ions. The DIA-generated MS/MS spectra present a formidable obstacle due to their inherent high multiplexing nature. Each spectrum encapsulates fragmented product ions originating from multiple precursor peptides. This intricacy poses a particularly acute challenge in de novo peptide/protein sequencing, where current methods are ill-equipped to address the multiplexing conundrum. In this paper, we introduce Transformer-DIA, a deep-learning model based on transformer architecture. It deciphers peptide sequences from DIA mass spectrometry data. Our results show significant improvements over existing STOA methods, including DeepNovo-DIA and PepNet. Transformer-DIA enhances precision by 15.14% to 34.8%, recall by 11.62% to 31.94% at the amino acid level, and boosts precision by 59% to 81.36% at the peptide level. Integrating DIA data and our Transformer-DIA model holds considerable promise to uncover novel peptides and more comprehensive profiling of biological samples. Transformer-DIA is freely available under the GNU GPL license at https//github.com/Biocomputing-Research-Group/Transformer-DIA.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article